levetiracetam

Generic: levetiracetam

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

levetiracetam 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-9847
Product ID 63629-9847_cac0490d-b164-41d1-81f9-336c8cf1b5b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203468
Listing Expiration 2026-12-31
Marketing Start 2014-05-01

Pharmacologic Class

Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636299847
Hyphenated Format 63629-9847

Supplemental Identifiers

RxCUI
807832
UNII
44YRR34555
NUI
N0000008486

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name levetiracetam (source: ndc)
Generic Name levetiracetam (source: ndc)
Application Number ANDA203468 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 21 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-1)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-2)
source: ndc

Packages (2)

Ingredients (1)

levetiracetam (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cac0490d-b164-41d1-81f9-336c8cf1b5b9", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["807832"], "spl_set_id": ["ace53552-d616-45e8-9f99-2f0041d0b430"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-1)", "package_ndc": "63629-9847-1", "marketing_start_date": "20230927"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9847-2)", "package_ndc": "63629-9847-2", "marketing_start_date": "20240709"}], "brand_name": "LEVETIRACETAM", "product_id": "63629-9847_cac0490d-b164-41d1-81f9-336c8cf1b5b9", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-9847", "generic_name": "LEVETIRACETAM", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVETIRACETAM", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA203468", "marketing_category": "ANDA", "marketing_start_date": "20140501", "listing_expiration_date": "20261231"}